Several N-lactosylated aryl thioureas and benzothiazolyl thioureas have been prepared by the condensation of hepta-O-acetyl-β-D-lactosyl isothiocyanate with aryl amines and 2-aminobenzothiazole/substituted benzothiazoles. Hepta-O-acetyl-β-D-lactosyl isothiocyanate was prepared by the interaction of hepta-O-acetyl-α-D-lactosyl bromide and lead thiocyanate. The structures of these new N-lactosides have been established on the basis of IR, NMR, and mass spectral studies. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:306–309, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20207

中文翻译：

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N-乳糖基化硫脲和苯并噻唑基硫脲的合成

通过七-O-乙酰基-β-D-乳糖基异硫氰酸酯与芳基胺和2-氨基苯并噻唑/取代苯并噻唑的缩合，已经制备了几种N-乳糖基化芳基硫脲和苯并噻唑基硫脲。七-O-乙酰基-β-D-乳糖基异硫氰酸酯是由七-O-乙酰基-α-D-乳糖基溴化物和硫氰酸铅相互作用制备的。这些新的 N-乳糖苷的结构是在红外、核磁共振和质谱研究的基础上建立的。© 2006 Wiley Periodicals, Inc. 杂原子化学 17:306–309, 2006; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.20207